As a method for diagnosing jaundice of a user based on an image by a jaundice diagnosis device, a jaundice diagnosis image is obtained including a jaundice diagnosis reference device divided into a first area and a second area, and a specific body part of a user located in the first area. The identification information of the jaundice diagnosis reference device inserted in the second area is extracted, and validity authentication of the identification information is requested through an interlocked authentication system. When the validity authentication success message is received from the authentication system, the user is diagnosed with jaundice based on the image of a specific body part located in the first area and the jaundice diagnosis comparison image included in the second area.

Some embodiments provide a method for magnetic resonance imaging of polysaccharide molecules, that includes providing a magnetic field that is sufficiently homogeneous over an imaging volume, generating a spatial encoding in the magnetic field, and acquiring one or more water proton signal intensity measurements at each of multiple voxels within the imaging volume. The signal intensity measurements are acquired at one or more irradiation frequencies at lower parts-per-million (ppm) than a baseline frequency associated with free water protons. The method includes generating, based on the water proton signal intensity measurements in each voxel, a water proton signal intensity map of the relayed Nuclear Overhauser Effect (rNOE) exchange process of aliphatic protons in the polysaccharide molecules to free water protons in the imaging volume, and generating, using a calibration of the water proton signal intensity measurements for the rNOE exchange process, a concentration map of the polysaccharide molecules in the imaging volume.

The present disclosure deals with the quickening of MRI examinations. Subjects of the present disclosure are a method, a system, a computer program product, a use, a contrast agent for use and a kit.

A method and a device for selecting a detection area and an elasticity detection system. The method comprises: dividing organ tissue information to be recognized into a plurality of detection sub-areas, and calculating a feature value of the organ tissue information in the detection sub-area; determining an organ tissue boundary area according to the organ tissue information to be recognized; and determining an organ tissue boundary area according to the organ tissue boundary area and a preset feature value condition. The method can determine the organ tissue boundary according to the organ tissue information, and automatically adjust the detection area according to the organ tissue boundary.

An automatic classification method for distinguishing between indolent and clinically significant carcinoma using multiparametric MRI (mp-MRI) imaging is provided. By utilizing a convolutional neural network (CNN), which automatically extracts deep features, the hierarchical classification framework avoids deficiencies in current schemes in the art such as the need to provide handcrafted features predefined by a domain expert and the precise delineation of lesion boundaries by a human or computerized algorithm. This hierarchical classification framework is trained using previously acquired mp-MRI data with known cancer classification characteristics and the framework is applied to mp-MRI images of new patients to provide identification and computerized cancer classification results of a suspicious lesion.

Systems and methods are provided for neuro stimulation. In one implementation, a system is provided that includes a stimulator introduced into tissue at a target location and a central controller that communicates wirelessly with the stimulator. The stimulator includes a power system that receives wireless energy transmission, and an electrode system that transmits an electrical pulse for stimulating the target location. The central controller includes a power system that wirelessly delivers power to the stimulator, a communication system that wirelessly communicates with the stimulator, and a processing system that controls the power system and the communication system. The central controller may instruct the stimulator to transmit one or more electrical pulses to the target location to affect an endocrine function (e.g., affect the glucose level of a patient).

A control section as a tissue identification device includes: an absorbance ratio calculating section configured to calculate the ratio of an absorbance indicated by a transmitted portion of first inspection light transmitted through biological tissue to an absorbance indicated by a transmitted portion of second inspection light transmitted through the biological tissue; and an identification information generating section configured to generate identification information indicative of the type or state of the biological tissue by determining within which of a plurality of preset numerical ranges the ratio falls.

In a method for generating a surrogate marker based on medical image data mapping an image region, the medical image data is detected using a first interface, a first subregion of the image region is selected by segmenting a first structure included in the image region, a first property of the first subregion is extracted, the surrogate marker is determined based on the first property, and the surrogate marker is provided using a second interface.

Methods, systems, and apparatuses are described causing light to be emitted, causing a frequency at which the light is emitted to vary, receiving, based on the frequency variation, a user input, determining a critical flicker frequency (CFF) corresponding to the user input, and determining, based on the CFF, a disease state.

The present is directed to systems for ex vivo testing performance of a hemostatic or sealing product attached to an animal organ and fully covering a cored channel in said organ, comprising: a pressure sensor positioned proximate to said hemostatic or sealing product in said cored channel; a monitoring or recording device configured to receive pressure readings from said pressure sensor; and a pressurized fluid source connected to said cored channel and configured to supply said pressurized fluid into said cored channel under constant or variable pressure. The present invention is also directed to methods of use for such systems.